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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170602Generated: November 1, 2026

1,10-Phenanthroline → 2-(3-Bromophenyl)benzoxazole

https://huagongshe.com/reaction/2170602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantCesium carbonateHCID 10796—
Reactant2-BromoanilineHCID 11992—
ReactantBenzoyl chloride, 3-bromo-HCID 74377—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product2-(3-Bromophenyl)benzoxazoleHCID 870520100%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3-bromobenzoyl chloride (6.005 g, 27.36 mmol), 2-bromoaniline (4.707 g, 27.36 mmol), Cs2CO3 (17.83 g, 54.73 mmol), CuI (0.261 g, 1.37 mmol), 1,10-phenanthroline (0.493 g, 2.74 mmol) and anhydrous 1,4-dioxane (50 mL) was degassed with argon at 40° C. for 30 min while stirring. The reaction mixture was then maintained under argon at 120° C. while stirring until TLC (SiO2, 4:1 hexanes-ethyl acetate) confirmed consumption of the starting material (24 h). Upon cooling to RT, the mixture was filtered and the filtrant washed copiously with ethyl acetate (ca. 350 mL). The filtrate was then washed with sat. NaHCO3, H2O and brine, dried over MgSO4, filter and concentrated in vacuo. Purification of the crude product via flash chromatography (SiO2, 4:1-hexanes:ethyl acetate) afforded 2-(3-bromophenyl)benzo[d]oxazole (7.50 g, 100%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051284B2
Source datasetuspto-grants-2015_06
ORD IDord-40eeae8cc7ee4c2b9c8cc49a4cfbd4d1
Source noteuspto-grants-2015_06